Canonical Allele Identifier: PA2827007549
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala626Thr
CA10583300
NM_001318829.2:c.1876G>A